Allele Registry

Canonical Allele Identifier: PA2825031666

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002446155

ClinVar Variation:

1789007

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Leu762Arg	CA382539687 NM_000051.4:c.2285T>G